摘要
A microfluidic chip based method utilized for effective screening of high-throughput peptide libraries was achieved. Continuous flow bead trapping, sorting, arraying and in situ sequencing was integrated. Peptide library screening with 105 beads was processed within 4 hours and peptide ligands toward the target protein AHA and APN were successfully discovered.
源语言 | 英语 |
---|---|
页(从-至) | 61767-61770 |
页数 | 4 |
期刊 | RSC Advances |
卷 | 4 |
期 | 106 |
DOI | |
出版状态 | 已出版 - 2014 |
已对外发布 | 是 |